Uchida 2019.
| Study characteristics | |||
| Patient Sampling |
Inclusion/exclusion criteria Inclusion criteria: primary glioblastoma. Tested by FISH Prior testing Presumably histopathological diagnosis, although this was not explicitly reported. |
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| Patient characteristics and setting |
Number of participants/tumours with results for 1p/19q status by ≥ 2 DNA‐based tests: 141 Country: Japan Population source and setting: The Department of Neurosurgery, University of Kagoshima. 2009–2016 Age: NR Gender: NR Karnofsky performance status: NR First diagnosis/recurrent disease: unclear. Primary GBM |
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| Index tests |
2 tests: FISH (variant 1) and FISH (variant 2) FISH (variant 1) Tumour sample type: NR Region(s) analysed: 1p36/1q25, 19p13/19q13 (Vysis LSI DNA probes) Cut‐off: 20%. Criteria for judging whether a deletion was present: signals of 1p or 19q < signals of 1q or 19p. FISH (variant 2) Tumour sample type: NR Region(s) analysed: 1p36/1q25, 19p13/19q13 (Vysis LSI DNA probes) Cut‐off: 20%. Criteria for judging whether a deletion was present: single signal of 1p or 19q and 2 signals of 1q or 19p. |
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| Target condition and reference standard(s) | Target condition was absolute 1p/19q deletion. No tests used as reference standard in our analyses. | ||
| Flow and timing | This was 1 test analysed with 2 different cut‐offs. | ||
| Comparative | |||
| Notes | Conference abstract | ||
| Methodological quality | |||
| Item | Authors' judgement | Risk of bias | Applicability concerns |
| DOMAIN 1: Patient Selection | |||
| Was a consecutive or random sample of patients enrolled? | Unclear | ||
| Was a case‐control design avoided? | Yes | ||
| Did the study avoid inappropriate exclusions? | Unclear | ||
| Could the selection of patients have introduced bias? | Unclear risk | ||
| Are there concerns that the included patients and setting do not match the review question? | High | ||
| DOMAIN 2: Index Test (NanoString) | |||
| DOMAIN 2: Index Test (aCGH) | |||
| DOMAIN 2: Index Test (NGS) | |||
| DOMAIN 2: Index Test (G‐banding) | |||
| DOMAIN 2: Index Test (FISH (variant 4)) | |||
| DOMAIN 2: Index Test (SNP array) | |||
| DOMAIN 2: Index Test (PCR (with comparison to normal DNA)) | |||
| DOMAIN 2: Index Test (PCR (without comparison to normal DNA)) | |||
| DOMAIN 2: Index Test (CISH) | |||
| DOMAIN 2: Index Test (MS) | |||
| DOMAIN 2: Index Test (RFLP) | |||
| DOMAIN 2: Index Test (PCR‐based LOH) | |||
| DOMAIN 2: Index Test (NGS or aCGH (or both)) | |||
| DOMAIN 2: Index Test (Methylation array) | |||
| DOMAIN 2: Index Test (FISH) | |||
| DOMAIN 2: Index Test (FISH (variant 1)) | |||
| If a threshold was used, was it pre‐specified? | No | ||
| Were the index test results interpreted without knowledge of the results of the other tests being compared? | Unclear | ||
| Could the conduct or interpretation of the index test have introduced bias? | High risk | ||
| Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
| DOMAIN 2: Index Test (FISH (variant 2)) | |||
| If a threshold was used, was it pre‐specified? | No | ||
| Were the index test results interpreted without knowledge of the results of the other tests being compared? | Unclear | ||
| Could the conduct or interpretation of the index test have introduced bias? | High risk | ||
| Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
| DOMAIN 2: Index Test (FISH (variant 3)) | |||
| DOMAIN 2: Index Test (Real‐time PCR) | |||
| DOMAIN 2: Index Test (MLPA) | |||
| DOMAIN 2: Index Test (CGH) | |||
| DOMAIN 3: Reference Standard | |||
| Is the reference standards likely to correctly classify the target condition? | No | ||
| Could the reference standard, its conduct, or its interpretation have introduced bias? | High risk | ||
| Are there concerns that the target condition as defined by the reference standard does not match the question? | Low concern | ||
| DOMAIN 4: Flow and Timing | |||
| Was there an appropriate interval between index test and reference standard? | Yes | ||
| Were all patients included in the analysis? | Unclear | ||
| Could the patient flow have introduced bias? | Unclear risk | ||